Biocatalytic asymmetric hydrogen transfer

168Citations
Citations of this article
68Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Celling chemistry: Ketones (secondary alcohols) can be biocatalytically reduced (oxidized) at a substrate concentration of up to 1.8 mol L-1 in an asymmetric fashion by employing a novel secondary alcohol dehydrogenase from Rhodococcus ruber DSM 44541 (see scheme). Furthermore, the enzyme is exceptionally stable at high cosubstrate concentrations, that is, 2-propanol (50% v/v) for reduction and acetone (20% v/v) for oxidation, respectively.

Cite

CITATION STYLE

APA

Stampfer, W., Kosjek, B., Moitzi, C., Kroutil, W., & Faber, K. (2002). Biocatalytic asymmetric hydrogen transfer. Angewandte Chemie - International Edition, 41(6), 1014–1017. https://doi.org/10.1002/1521-3773(20020315)41:6<1014::AID-ANIE1014>3.0.CO;2-6

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free